Bromide

Bromide

SCHEMBL22323918

CCCCCOc1ccccc1C(=O)Nc1ccc(C(=O)OCC[N+](C)(CC)CC)cc1.[Br-]

nearest known ligand 0.98

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

The experimentally established mechanism targets of Bromide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHRM2 known ✓ P08172 1/20 0.98
CHRM1 known ✓ P11229 1/20 0.98
CHRM3 known ✓ P20309 1/20 0.98
MLNR O43193 1/20 0.98
NR1I2 O75469 1/20 0.98
NR3C1 P04150 1/20 0.98
PGR P06401 1/20 0.98
ADRB2 P07550 1/20 0.98
ADRB1 P08588 1/20 0.98
HTR1A P08908 1/20 0.98
ADORA3 P0DMS8 1/20 0.98
DRD2 P14416 1/20 0.98
ADRA2B P18089 1/20 0.98
ADRA2C P18825 1/20 0.98
CNR1 P21554 1/20 0.98
SLC6A2 P23975 1/20 0.98
NPY1R P25929 1/20 0.98
HTR2A P28223 1/20 0.98
HTR2C P28335 1/20 0.98
ADORA2A P29274 1/20 0.98

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Otilonium SCHEMBL109554 0.99 NR1I2 (1.00) MLNRNR1I2NR3C1PGRADRB2
Bromide SCHEMBL22324597 0.99 NR1I2 (1.00) MLNRNR1I2NR3C1PGRADRB2
Bromide SCHEMBL22323864 0.99 NR1I2 (1.00) MLNRNR1I2NR3C1PGRADRB2
Bromide SCHEMBL22324509 0.99 NR1I2 (1.00) MLNRNR1I2NR3C1PGRADRB2
Bromide SCHEMBL22323721 0.99 NR1I2 (1.00) MLNRNR1I2NR3C1PGRADRB2
Bromide SCHEMBL22324633 0.99 NR1I2 (1.00) MLNRNR1I2NR3C1PGRADRB2
Bromide SCHEMBL22324511 0.99 NR1I2 (1.00) MLNRNR1I2NR3C1PGRADRB2
Bromide SCHEMBL22324606 0.99 NR1I2 (1.00) MLNRNR1I2NR3C1PGRADRB2
Bromide SCHEMBL22323711 0.99 NR1I2 (1.00) MLNRNR1I2NR3C1PGRADRB2
Otilonium SCHEMBL31646954 0.98 KMT2A (1.00) MLNRNR1I2NR3C1PGRADRB2

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 3 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11952330-B2 Antibiotic ammonium compounds and methods for the treatment of bacterial infections BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2024-04-09 US disclosed
US-20220098148-A1 ANTIBIOTIC AMMONIUM COMPOUNDS AND METHODS FOR THE TREATMENT OF BACTERIAL INFECTIONS BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2022-03-31 US disclosed
WO-2020163479-A1 ANTIBIOTIC AMMONIUM COMPOUNDS AND METHODS FOR THE TREATMENT OF BACTERIAL INFECTIONS BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 2020-08-13 WO disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (2 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20220098148-A1 ANTIBIOTIC AMMONIUM COMPOUNDS AND METHODS FOR THE TREATMENT OF BACTERIAL INFECTIONS ARG1, SLC10A2, ALPI CHRM2 4733/4885CHRM1 4159/4885CHRM3 4773/4885
US-11952330-B2 Antibiotic ammonium compounds and methods for the treatment of bacterial infections ARG1, SLC10A2, ALPI CHRM2 4733/4885CHRM1 4159/4885CHRM3 4773/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.